A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1674268



Internal ID15531776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63542268..63718326hg38UCSC Ensembl
Innerchr9:68138002..68314060hg19UCSC Ensembl
Innerchr9:67627822..67803880hg18UCSC Ensembl
Innerchr9:64805732..64981790hg16UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38176059
hg19176059
hg18176059
hg16176059
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469763
Supporting Variants
Samples
Known Genes
MethodBAC aCGH
AnalysisA locus was considered a CNV if the log ratio of fluorescence measurements for the individuals assayed exceeded twice the SD of the autosomal clones in both dye-swapped experiments.
PlatformGPL4010
Comments
ReferenceLocke_et_al_2006
Pubmed ID16826518
Accession Number(s)nssv1674268
Frequency
Sample Size265
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer